| 15192570 | CV721259 | single nucleotide variant | NM_018926.3(PCDHGB6):c.199C>A (p.Arg67=) | not provided [RCV000888699] | benign | 5 | 141408401 | 141408401 | Human | | name |
| 156182632 | CV2243096 | single nucleotide variant | NM_018926.3(PCDHGB6):c.83C>T (p.Thr28Ile) | not specified [RCV004110007] | uncertain significance | 5 | 141408285 | 141408285 | Human | | name |
| 405760261 | CV3364505 | single nucleotide variant | NM_018926.3(PCDHGB6):c.92A>G (p.Glu31Gly) | not specified [RCV004500520] | uncertain significance | 5 | 141408294 | 141408294 | Human | | name |
| 156265170 | CV2198635 | single nucleotide variant | NM_018926.3(PCDHGB6):c.286T>C (p.Cys96Arg) | not specified [RCV004075649] | uncertain significance | 5 | 141408488 | 141408488 | Human | | name |
| 156338855 | CV2271338 | single nucleotide variant | NM_018926.3(PCDHGB6):c.107C>T (p.Ser36Leu) | not specified [RCV004136455] | uncertain significance | 5 | 141408309 | 141408309 | Human | | name |
| 156254416 | CV2359209 | single nucleotide variant | NM_018926.3(PCDHGB6):c.286T>G (p.Cys96Gly) | not specified [RCV004212504] | uncertain significance | 5 | 141408488 | 141408488 | Human | | name |
| 156176992 | CV2374490 | single nucleotide variant | NM_018926.3(PCDHGB6):c.244G>A (p.Gly82Arg) | not specified [RCV004231995] | uncertain significance | 5 | 141408446 | 141408446 | Human | | name |
| 401881397 | CV2789599 | single nucleotide variant | NM_018926.3(PCDHGB6):c.119A>G (p.Glu40Gly) | not specified [RCV004360201] | uncertain significance | 5 | 141408321 | 141408321 | Human | | name |
| 401917956 | CV2825350 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1146C>T (p.Val382=) | not provided [RCV003429852] | likely benign | 5 | 141409348 | 141409348 | Human | | name |
| 401915192 | CV2825351 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1962C>T (p.Leu654=) | not provided [RCV003428652] | likely benign | 5 | 141410164 | 141410164 | Human | | name |
| 401915197 | CV2825353 | single nucleotide variant | NM_018926.3(PCDHGB6):c.2268T>C (p.Ile756=) | not provided [RCV003428653] | likely benign | 5 | 141410470 | 141410470 | Human | | name |
| 405760198 | CV3364497 | single nucleotide variant | NM_018926.3(PCDHGB6):c.202G>C (p.Val68Leu) | not specified [RCV004500512] | uncertain significance | 5 | 141408404 | 141408404 | Human | | name |
| 407484958 | CV3459846 | single nucleotide variant | NM_018926.3(PCDHGB6):c.275G>A (p.Arg92His) | not specified [RCV004659524] | uncertain significance | 5 | 141408477 | 141408477 | Human | | name |
| 598195800 | CV3996412 | single nucleotide variant | NM_018926.3(PCDHGB6):c.235G>T (p.Ala79Ser) | not specified [RCV005397590] | uncertain significance | 5 | 141408437 | 141408437 | Human | | name |
| 598195808 | CV3996414 | single nucleotide variant | NM_018926.3(PCDHGB6):c.113C>T (p.Pro38Leu) | not specified [RCV005397591] | uncertain significance | 5 | 141408315 | 141408315 | Human | | name |
| 156240500 | CV2213645 | single nucleotide variant | NM_018926.3(PCDHGB6):c.509A>T (p.Tyr170Phe) | not specified [RCV004089725] | uncertain significance | 5 | 141408711 | 141408711 | Human | | name |
| 156339486 | CV2225095 | single nucleotide variant | NM_018926.3(PCDHGB6):c.574C>T (p.Pro192Ser) | not specified [RCV004094912] | uncertain significance | 5 | 141408776 | 141408776 | Human | | name |
| 156254962 | CV2229236 | single nucleotide variant | NM_018926.3(PCDHGB6):c.993T>G (p.Cys331Trp) | not specified [RCV004101049] | uncertain significance | 5 | 141409195 | 141409195 | Human | | name |
| 156061584 | CV2280435 | single nucleotide variant | NM_018926.3(PCDHGB6):c.676G>A (p.Ala226Thr) | not specified [RCV004140609] | uncertain significance | 5 | 141408878 | 141408878 | Human | | name |
| 156263859 | CV2364190 | single nucleotide variant | NM_018926.3(PCDHGB6):c.853G>A (p.Ala285Thr) | not specified [RCV004223429] | uncertain significance | 5 | 141409055 | 141409055 | Human | | name |
| 329367552 | CV2427439 | single nucleotide variant | NM_018926.3(PCDHGB6):c.560A>T (p.Asp187Val) | not specified [RCV004248291] | uncertain significance | 5 | 141408762 | 141408762 | Human | | name |
| 329373469 | CV2434262 | single nucleotide variant | NM_018926.3(PCDHGB6):c.532T>C (p.Phe178Leu) | not specified [RCV004251937] | uncertain significance | 5 | 141408734 | 141408734 | Human | | name |
| 329373881 | CV2452517 | single nucleotide variant | NM_018926.3(PCDHGB6):c.829A>G (p.Ile277Val) | not specified [RCV004273112] | uncertain significance | 5 | 141409031 | 141409031 | Human | | name |
| 329351575 | CV2462121 | single nucleotide variant | NM_018926.3(PCDHGB6):c.511A>G (p.Lys171Glu) | not specified [RCV004266146] | uncertain significance | 5 | 141408713 | 141408713 | Human | | name |
| 405760236 | CV3364502 | single nucleotide variant | NM_018926.3(PCDHGB6):c.478C>G (p.Pro160Ala) | not specified [RCV004500517] | uncertain significance | 5 | 141408680 | 141408680 | Human | | name |
| 405760244 | CV3364503 | single nucleotide variant | NM_018926.3(PCDHGB6):c.482A>T (p.Asp161Val) | not specified [RCV004500518] | uncertain significance | 5 | 141408684 | 141408684 | Human | | name |
| 405760252 | CV3364504 | single nucleotide variant | NM_018926.3(PCDHGB6):c.872T>C (p.Met291Thr) | not specified [RCV004500519] | uncertain significance | 5 | 141409074 | 141409074 | Human | | name |
| 405760277 | CV3364507 | single nucleotide variant | NM_018926.3(PCDHGB6):c.940A>G (p.Arg314Gly) | not specified [RCV004500522] | uncertain significance | 5 | 141409142 | 141409142 | Human | | name |
| 407484934 | CV3459841 | single nucleotide variant | NM_018926.3(PCDHGB6):c.665G>T (p.Arg222Ile) | not specified [RCV004659521] | uncertain significance | 5 | 141408867 | 141408867 | Human | | name |
| 407483568 | CV3459843 | single nucleotide variant | NM_018926.3(PCDHGB6):c.884A>G (p.Asp295Gly) | not specified [RCV004653303] | uncertain significance | 5 | 141409086 | 141409086 | Human | | name |
| 407483584 | CV3459847 | single nucleotide variant | NM_018926.3(PCDHGB6):c.668G>C (p.Ser223Thr) | not specified [RCV004653305] | uncertain significance | 5 | 141408870 | 141408870 | Human | | name |
| 407483602 | CV3459852 | single nucleotide variant | NM_018926.3(PCDHGB6):c.974G>A (p.Gly325Asp) | not specified [RCV004653307] | uncertain significance | 5 | 141409176 | 141409176 | Human | | name |
| 597739645 | CV3571624 | single nucleotide variant | NM_018926.3(PCDHGB6):c.655G>T (p.Asp219Tyr) | not specified [RCV004844208] | uncertain significance | 5 | 141408857 | 141408857 | Human | | name |
| 597739640 | CV3571625 | single nucleotide variant | NM_018926.3(PCDHGB6):c.358A>G (p.Ile120Val) | not specified [RCV004844209] | likely benign | 5 | 141408560 | 141408560 | Human | | name |
| 597739635 | CV3571626 | single nucleotide variant | NM_018926.3(PCDHGB6):c.670G>T (p.Ala224Ser) | not specified [RCV004844210] | uncertain significance | 5 | 141408872 | 141408872 | Human | | name |
| 597739630 | CV3571627 | single nucleotide variant | NM_018926.3(PCDHGB6):c.467C>T (p.Pro156Leu) | not specified [RCV004844211] | uncertain significance | 5 | 141408669 | 141408669 | Human | | name |
| 598271119 | CV3996413 | single nucleotide variant | NM_018926.3(PCDHGB6):c.839A>G (p.Tyr280Cys) | not specified [RCV005389107] | uncertain significance | 5 | 141409041 | 141409041 | Human | | name |
| 598271124 | CV3996416 | single nucleotide variant | NM_018926.3(PCDHGB6):c.842T>C (p.Phe281Ser) | not specified [RCV005389108] | uncertain significance | 5 | 141409044 | 141409044 | Human | | name |
| 598271141 | CV3996419 | single nucleotide variant | NM_018926.3(PCDHGB6):c.778C>T (p.Pro260Ser) | not specified [RCV005389111] | likely benign | 5 | 141408980 | 141408980 | Human | | name |
| 156374162 | CV2198275 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1425C>A (p.Ser475Arg) | not specified [RCV004081831] | uncertain significance | 5 | 141409627 | 141409627 | Human | | name |
| 156179330 | CV2201650 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1601C>G (p.Ala534Gly) | not specified [RCV004082110] | uncertain significance | 5 | 141409803 | 141409803 | Human | | name |
| 156368072 | CV2203649 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1411A>G (p.Ile471Val) | not specified [RCV004073966] | uncertain significance | 5 | 141409613 | 141409613 | Human | | name |
| 155981374 | CV2244071 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1603C>A (p.Arg535Ser) | not specified [RCV004108550] | uncertain significance | 5 | 141409805 | 141409805 | Human | | name |
| 156164367 | CV2246780 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1519G>A (p.Val507Met) | not specified [RCV004112312] | uncertain significance | 5 | 141409721 | 141409721 | Human | | name |
| 156184861 | CV2251615 | single nucleotide variant | NM_018926.3(PCDHGB6):c.2375A>G (p.His792Arg) | not specified [RCV004117848] | uncertain significance | 5 | 141410577 | 141410577 | Human | | name |
| 156236013 | CV2268078 | single nucleotide variant | NM_018926.3(PCDHGB6):c.2369C>T (p.Pro790Leu) | not specified [RCV004138408] | uncertain significance | 5 | 141410571 | 141410571 | Human | | name |
| 156064758 | CV2287205 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1345G>T (p.Ala449Ser) | not specified [RCV004146855] | uncertain significance | 5 | 141409547 | 141409547 | Human | | name |
| 156262066 | CV2287562 | single nucleotide variant | NM_018926.3(PCDHGB6):c.2186C>A (p.Pro729His) | not specified [RCV004141012] | uncertain significance | 5 | 141410388 | 141410388 | Human | | name |
| 156097201 | CV2310247 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1781T>C (p.Val594Ala) | not specified [RCV004163344] | uncertain significance | 5 | 141409983 | 141409983 | Human | | name |
| 155976050 | CV2338550 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1114C>T (p.Arg372Trp) | not specified [RCV004189005] | uncertain significance | 5 | 141409316 | 141409316 | Human | | name |
| 329374540 | CV2443927 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1731G>A (p.Met577Ile) | not specified [RCV004258257] | uncertain significance | 5 | 141409933 | 141409933 | Human | | name |
| 329378661 | CV2463677 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1983T>A (p.His661Gln) | not specified [RCV004279253] | uncertain significance | 5 | 141410185 | 141410185 | Human | | name |
| 401754091 | CV2685160 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1339G>C (p.Asp447His) | not specified [RCV004289723] | uncertain significance | 5 | 141409541 | 141409541 | Human | | name |
| 401733626 | CV2713157 | single nucleotide variant | NM_018926.3(PCDHGB6):c.2084C>T (p.Ala695Val) | not specified [RCV004316705] | uncertain significance | 5 | 141410286 | 141410286 | Human | | name |
| 401764522 | CV2721347 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1357G>C (p.Asp453His) | not specified [RCV004322101] | likely benign | 5 | 141409559 | 141409559 | Human | | name |
| 401874504 | CV2774006 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1070T>G (p.Leu357Trp) | not specified [RCV004358414] | uncertain significance | 5 | 141409272 | 141409272 | Human | | name |
| 401862948 | CV2775362 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1057T>C (p.Ser353Pro) | not specified [RCV004348767] | uncertain significance | 5 | 141409259 | 141409259 | Human | | name |
| 401917958 | CV2825352 | single nucleotide variant | NM_018926.3(PCDHGB6):c.2252C>T (p.Ser751Phe) | not provided [RCV003429853] | likely benign | 5 | 141410454 | 141410454 | Human | | name |
| 405866973 | CV2842515 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1921C>T (p.Arg641Cys) | EBV-positive nodal T- and NK-cell lymphoma [RCV004557872] | likely benign | 5 | 141410123 | 141410123 | Human | | name |
| 405760179 | CV3364494 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1295T>G (p.Leu432Arg) | not specified [RCV004500509] | uncertain significance | 5 | 141409497 | 141409497 | Human | | name |
| 405760185 | CV3364495 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1372G>C (p.Val458Leu) | not specified [RCV004500510] | likely benign | 5 | 141409574 | 141409574 | Human | | name |
| 405760192 | CV3364496 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1624C>T (p.Leu542Phe) | not specified [RCV004500511] | uncertain significance | 5 | 141409826 | 141409826 | Human | | name |
| 405760204 | CV3364498 | single nucleotide variant | NM_018926.3(PCDHGB6):c.2131A>G (p.Ile711Val) | not specified [RCV004500513] | likely benign | 5 | 141410333 | 141410333 | Human | | name |
| 405760214 | CV3364499 | single nucleotide variant | NM_018926.3(PCDHGB6):c.2222C>A (p.Pro741His) | not specified [RCV004500514] | uncertain significance | 5 | 141410424 | 141410424 | Human | | name |
| 405760220 | CV3364500 | single nucleotide variant | NM_018926.3(PCDHGB6):c.2255A>G (p.Tyr752Cys) | not specified [RCV004500515] | uncertain significance | 5 | 141410457 | 141410457 | Human | | name |
| 405760229 | CV3364501 | single nucleotide variant | NM_018926.3(PCDHGB6):c.2273A>T (p.His758Leu) | not specified [RCV004500516] | uncertain significance | 5 | 141410475 | 141410475 | Human | | name |
| 407484943 | CV3459842 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1362G>C (p.Gln454His) | not specified [RCV004659522] | uncertain significance | 5 | 141409564 | 141409564 | Human | | name |
| 407483576 | CV3459844 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1649T>C (p.Val550Ala) | not specified [RCV004653304] | uncertain significance | 5 | 141409851 | 141409851 | Human | | name |
| 407484952 | CV3459845 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1397C>A (p.Pro466Gln) | not specified [RCV004659523] | uncertain significance | 5 | 141409599 | 141409599 | Human | | name |
| 407483593 | CV3459848 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1861C>A (p.Leu621Met) | not specified [RCV004653306] | uncertain significance | 5 | 141410063 | 141410063 | Human | | name |
| 407484966 | CV3459849 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1502T>C (p.Val501Ala) | not specified [RCV004659525] | uncertain significance | 5 | 141409704 | 141409704 | Human | | name |
| 407484974 | CV3459850 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1811T>A (p.Leu604Gln) | not specified [RCV004659526] | uncertain significance | 5 | 141410013 | 141410013 | Human | | name |
| 597739050 | CV3571622 | single nucleotide variant | NM_018926.3(PCDHGB6):c.2029G>A (p.Asp677Asn) | not specified [RCV004844206] | uncertain significance | 5 | 141410231 | 141410231 | Human | | name |
| 597739651 | CV3571623 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1742C>T (p.Ser581Phe) | not specified [RCV004844207] | uncertain significance | 5 | 141409944 | 141409944 | Human | | name |
| 597739624 | CV3571629 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1648G>A (p.Val550Met) | not specified [RCV004844212] | uncertain significance | 5 | 141409850 | 141409850 | Human | | name |
| 597756520 | CV3571630 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1436C>T (p.Pro479Leu) | not specified [RCV004848139] | uncertain significance | 5 | 141409638 | 141409638 | Human | | name |
| 597739619 | CV3571631 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1789G>T (p.Asp597Tyr) | not specified [RCV004844213] | uncertain significance | 5 | 141409991 | 141409991 | Human | | name |
| 597739614 | CV3571632 | single nucleotide variant | NM_018926.3(PCDHGB6):c.2371C>T (p.Pro791Ser) | not specified [RCV004844214] | uncertain significance | 5 | 141410573 | 141410573 | Human | | name |
| 598195814 | CV3996415 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1603C>T (p.Arg535Cys) | not specified [RCV005397592] | uncertain significance | 5 | 141409805 | 141409805 | Human | | name |
| 598271130 | CV3996417 | single nucleotide variant | NM_018926.3(PCDHGB6):c.1800C>A (p.His600Gln) | not specified [RCV005389109] | uncertain significance | 5 | 141410002 | 141410002 | Human | | name |
| 598271137 | CV3996418 | single nucleotide variant | NM_018926.3(PCDHGB6):c.2248T>A (p.Tyr750Asn) | not specified [RCV005389110] | uncertain significance | 5 | 141410450 | 141410450 | Human | | name |
