| 401923975 | CV2821048 | single nucleotide variant | NM_145004.7(ADAM32):c.186G>A (p.Val62=) | not provided [RCV003435469] | likely benign | 8 | 39136704 | 39136704 | Human | | name |
| 405781123 | CV3306775 | single nucleotide variant | NM_145004.7(ADAM32):c.20T>C (p.Leu7Pro) | not specified [RCV004436972] | uncertain significance | 8 | 39107795 | 39107795 | Human | | name |
| 405693301 | CV3226534 | microsatellite | NM_145004.6(ADAM32):c.-69_-62CGCGTCCC[3] | not provided [RCV003992927] | likely benign | 8 | 39107706 | 39107707 | Human | | name |
| 405781449 | CV3300957 | single nucleotide variant | NM_145004.7(ADAM32):c.85G>A (p.Val29Ile) | not specified [RCV004437026] | likely benign | 8 | 39118112 | 39118112 | Human | | name |
| 401861222 | CV2758810 | single nucleotide variant | NM_145004.7(ADAM32):c.149C>G (p.Ser50Cys) | not specified [RCV004337862] | uncertain significance | 8 | 39136667 | 39136667 | Human | | name |
| 401856096 | CV2764341 | single nucleotide variant | NM_145004.7(ADAM32):c.2280A>G (p.Lys760=) | not specified [RCV004338914] | likely benign | 8 | 39281136 | 39281136 | Human | | name |
| 401909199 | CV2821049 | single nucleotide variant | NM_145004.7(ADAM32):c.1074T>A (p.Thr358=) | not provided [RCV003423911] | likely benign | 8 | 39211165 | 39211165 | Human | | name |
| 156079855 | CV2226576 | single nucleotide variant | NM_145004.7(ADAM32):c.644A>T (p.Glu215Val) | not specified [RCV004101831] | uncertain significance | 8 | 39164813 | 39164813 | Human | | name |
| 156204366 | CV2252476 | single nucleotide variant | NM_145004.7(ADAM32):c.358A>G (p.Ile120Val) | not specified [RCV004116595] | uncertain significance | 8 | 39151381 | 39151381 | Human | | name |
| 155964353 | CV2282830 | single nucleotide variant | NM_145004.7(ADAM32):c.893G>A (p.Arg298His) | not provided [RCV004704889]|not specified [RCV004143491] | likely benign | 8 | 39169975 | 39169975 | Human | | name |
| 156345816 | CV2291220 | single nucleotide variant | NM_145004.7(ADAM32):c.562C>A (p.Leu188Ile) | not specified [RCV004153513] | uncertain significance | 8 | 39160933 | 39160933 | Human | | name |
| 156071246 | CV2325184 | single nucleotide variant | NM_145004.7(ADAM32):c.593T>C (p.Leu198Ser) | not specified [RCV004177601] | uncertain significance | 8 | 39160964 | 39160964 | Human | | name |
| 329382714 | CV2424531 | single nucleotide variant | NM_145004.7(ADAM32):c.637G>A (p.Val213Ile) | not specified [RCV004254033] | likely benign | 8 | 39164806 | 39164806 | Human | | name |
| 329391719 | CV2453063 | single nucleotide variant | NM_145004.7(ADAM32):c.826C>A (p.Leu276Ile) | not specified [RCV004277673] | uncertain significance | 8 | 39165189 | 39165189 | Human | | name |
| 329401895 | CV2457496 | single nucleotide variant | NM_145004.7(ADAM32):c.629C>G (p.Thr210Arg) | not specified [RCV004267310] | uncertain significance | 8 | 39164798 | 39164798 | Human | | name |
| 401773517 | CV2695270 | single nucleotide variant | NM_145004.7(ADAM32):c.460G>A (p.Ala154Thr) | not specified [RCV004303400] | uncertain significance | 8 | 39151483 | 39151483 | Human | | name |
| 401775852 | CV2706780 | single nucleotide variant | NM_145004.7(ADAM32):c.987A>G (p.Ile329Met) | not specified [RCV004319633] | uncertain significance | 8 | 39186980 | 39186980 | Human | | name |
| 405781253 | CV3300924 | single nucleotide variant | NM_145004.7(ADAM32):c.578T>C (p.Val193Ala) | not specified [RCV004436993] | uncertain significance | 8 | 39160949 | 39160949 | Human | | name |
| 405781289 | CV3300929 | single nucleotide variant | NM_145004.7(ADAM32):c.580G>A (p.Val194Met) | not specified [RCV004436998] | uncertain significance | 8 | 39160951 | 39160951 | Human | | name |
| 405781479 | CV3300962 | single nucleotide variant | NM_145004.7(ADAM32):c.872C>T (p.Pro291Leu) | not specified [RCV004437031] | uncertain significance | 8 | 39169954 | 39169954 | Human | | name |
| 597738726 | CV3648336 | single nucleotide variant | NM_145004.7(ADAM32):c.812A>T (p.His271Leu) | not specified [RCV004890179] | uncertain significance | 8 | 39165175 | 39165175 | Human | | name |
| 597778310 | CV3648354 | single nucleotide variant | NM_145004.7(ADAM32):c.783G>C (p.Trp261Cys) | not specified [RCV004898985] | uncertain significance | 8 | 39165146 | 39165146 | Human | | name |
| 597778606 | CV3648372 | single nucleotide variant | NM_145004.7(ADAM32):c.925G>A (p.Glu309Lys) | not specified [RCV004898999] | uncertain significance | 8 | 39186918 | 39186918 | Human | | name |
| 598228022 | CV3943452 | single nucleotide variant | NM_145004.7(ADAM32):c.916T>A (p.Tyr306Asn) | not specified [RCV005319018] | uncertain significance | 8 | 39186909 | 39186909 | Human | | name |
| 598192017 | CV3943473 | single nucleotide variant | NM_145004.7(ADAM32):c.623T>C (p.Ile208Thr) | not specified [RCV005312718] | uncertain significance | 8 | 39164792 | 39164792 | Human | | name |
| 598228055 | CV3943489 | single nucleotide variant | NM_145004.7(ADAM32):c.371A>C (p.Glu124Ala) | not specified [RCV005319024] | uncertain significance | 8 | 39151394 | 39151394 | Human | | name |
| 156110702 | CV2207699 | single nucleotide variant | NM_145004.7(ADAM32):c.2095G>A (p.Ala699Thr) | not specified [RCV004084148] | uncertain significance | 8 | 39257276 | 39257276 | Human | | name |
| 156031996 | CV2259461 | single nucleotide variant | NM_145004.7(ADAM32):c.2161G>A (p.Glu721Lys) | not specified [RCV004122665] | uncertain significance | 8 | 39257342 | 39257342 | Human | | name |
| 155900966 | CV2275295 | single nucleotide variant | NM_145004.7(ADAM32):c.1789A>G (p.Lys597Glu) | not specified [RCV004137070] | uncertain significance | 8 | 39234053 | 39234053 | Human | | name |
| 156027129 | CV2278408 | single nucleotide variant | NM_145004.7(ADAM32):c.1541C>T (p.Pro514Leu) | not specified [RCV004132867] | uncertain significance | 8 | 39232042 | 39232042 | Human | | name |
| 155903605 | CV2298647 | single nucleotide variant | NM_145004.7(ADAM32):c.2077A>G (p.Ile693Val) | not specified [RCV004162571] | likely benign | 8 | 39257258 | 39257258 | Human | | name |
| 156159806 | CV2322776 | single nucleotide variant | NM_145004.7(ADAM32):c.1703A>G (p.Asp568Gly) | not specified [RCV004182883] | uncertain significance | 8 | 39233967 | 39233967 | Human | | name |
| 156052776 | CV2336762 | single nucleotide variant | NM_145004.7(ADAM32):c.1316A>G (p.Lys439Arg) | not specified [RCV004196999] | likely benign | 8 | 39221692 | 39221692 | Human | | name |
| 156279265 | CV2338298 | single nucleotide variant | NM_145004.7(ADAM32):c.1862C>T (p.Ala621Val) | not specified [RCV004186353] | uncertain significance | 8 | 39246126 | 39246126 | Human | | name |
| 155921476 | CV2350673 | single nucleotide variant | NM_145004.7(ADAM32):c.1952C>A (p.Pro651Gln) | not specified [RCV004207022] | uncertain significance | 8 | 39254463 | 39254463 | Human | | name |
| 156155253 | CV2371226 | single nucleotide variant | NM_145004.7(ADAM32):c.1720G>A (p.Val574Ile) | not specified [RCV004220964] | uncertain significance | 8 | 39233984 | 39233984 | Human | | name |
| 156177388 | CV2374516 | single nucleotide variant | NM_145004.7(ADAM32):c.1811T>C (p.Ile604Thr) | not specified [RCV004232019] | likely benign | 8 | 39234075 | 39234075 | Human | | name |
| 329365587 | CV2440911 | single nucleotide variant | NM_145004.7(ADAM32):c.1984A>G (p.Ile662Val) | not specified [RCV004261301] | uncertain significance | 8 | 39254495 | 39254495 | Human | | name |
| 401726927 | CV2691902 | single nucleotide variant | NM_145004.7(ADAM32):c.1226C>T (p.Thr409Ile) | not specified [RCV004299641] | uncertain significance | 8 | 39211317 | 39211317 | Human | | name |
| 401746914 | CV2698734 | single nucleotide variant | NM_145004.7(ADAM32):c.1085G>A (p.Cys362Tyr) | not specified [RCV004301190] | uncertain significance | 8 | 39211176 | 39211176 | Human | | name |
| 401749369 | CV2706654 | single nucleotide variant | NM_145004.7(ADAM32):c.1502G>A (p.Arg501His) | not specified [RCV004319231] | uncertain significance | 8 | 39223215 | 39223215 | Human | | name |
| 401767890 | CV2729987 | single nucleotide variant | NM_145004.7(ADAM32):c.1342G>A (p.Val448Ile) | not specified [RCV004332975] | uncertain significance | 8 | 39223055 | 39223055 | Human | | name |
| 401861302 | CV2755532 | single nucleotide variant | NM_145004.7(ADAM32):c.1363C>T (p.His455Tyr) | not specified [RCV004340114] | uncertain significance | 8 | 39223076 | 39223076 | Human | | name |
| 401859814 | CV2768351 | single nucleotide variant | NM_145004.7(ADAM32):c.1174C>G (p.Pro392Ala) | not specified [RCV004350611] | uncertain significance | 8 | 39211265 | 39211265 | Human | | name |
| 401880363 | CV2783184 | single nucleotide variant | NM_145004.7(ADAM32):c.1532G>A (p.Arg511Lys) | not specified [RCV004363527] | likely benign | 8 | 39232033 | 39232033 | Human | | name |
| 405780587 | CV3306684 | single nucleotide variant | NM_145004.7(ADAM32):c.1130A>G (p.Lys377Arg) | not specified [RCV004436881] | likely benign | 8 | 39211221 | 39211221 | Human | | name |
| 405780708 | CV3306703 | single nucleotide variant | NM_145004.7(ADAM32):c.1342G>T (p.Val448Phe) | not specified [RCV004436900] | uncertain significance | 8 | 39223055 | 39223055 | Human | | name |
| 405780749 | CV3306710 | single nucleotide variant | NM_145004.7(ADAM32):c.1441C>T (p.Leu481Phe) | not specified [RCV004436907] | uncertain significance | 8 | 39223154 | 39223154 | Human | | name |
| 405780863 | CV3306730 | single nucleotide variant | NM_145004.7(ADAM32):c.1656A>C (p.Leu552Phe) | not specified [RCV004436927] | uncertain significance | 8 | 39233920 | 39233920 | Human | | name |
| 405780903 | CV3306737 | single nucleotide variant | NM_145004.7(ADAM32):c.1766C>G (p.Thr589Arg) | not specified [RCV004436934] | uncertain significance | 8 | 39234030 | 39234030 | Human | | name |
| 405780978 | CV3306750 | single nucleotide variant | NM_145004.7(ADAM32):c.1897C>T (p.His633Tyr) | not specified [RCV004436947] | uncertain significance | 8 | 39246161 | 39246161 | Human | | name |
| 405781023 | CV3306758 | single nucleotide variant | NM_145004.7(ADAM32):c.1985T>C (p.Ile662Thr) | not specified [RCV004436955] | uncertain significance | 8 | 39254496 | 39254496 | Human | | name |
| 405781040 | CV3306761 | single nucleotide variant | NM_145004.7(ADAM32):c.1996G>C (p.Glu666Gln) | not specified [RCV004436958] | uncertain significance | 8 | 39254507 | 39254507 | Human | | name |
| 405781160 | CV3306781 | single nucleotide variant | NM_145004.7(ADAM32):c.2324A>T (p.Lys775Ile) | not specified [RCV004436978] | uncertain significance | 8 | 39283591 | 39283591 | Human | | name |
| 407468650 | CV3428774 | single nucleotide variant | NM_145004.7(ADAM32):c.1132T>C (p.Cys378Arg) | not specified [RCV004614772] | uncertain significance | 8 | 39211223 | 39211223 | Human | | name |
| 407468675 | CV3428783 | single nucleotide variant | NM_145004.7(ADAM32):c.1073C>G (p.Thr358Ser) | not specified [RCV004614781] | uncertain significance | 8 | 39211164 | 39211164 | Human | | name |
| 407468691 | CV3428789 | single nucleotide variant | NM_145004.7(ADAM32):c.1898A>C (p.His633Pro) | not specified [RCV004614787] | uncertain significance | 8 | 39246162 | 39246162 | Human | | name |
| 597778128 | CV3648288 | single nucleotide variant | NM_145004.7(ADAM32):c.1154T>C (p.Met385Thr) | not specified [RCV004898942] | uncertain significance | 8 | 39211245 | 39211245 | Human | | name |
| 597778193 | CV3648306 | single nucleotide variant | NM_145004.7(ADAM32):c.1778C>T (p.Pro593Leu) | not specified [RCV004898957] | uncertain significance | 8 | 39234042 | 39234042 | Human | | name |
| 597778229 | CV3648316 | single nucleotide variant | NM_145004.7(ADAM32):c.2227A>G (p.Thr743Ala) | not specified [RCV004898965] | uncertain significance | 8 | 39274337 | 39274337 | Human | | name |
| 597778260 | CV3648328 | single nucleotide variant | NM_145004.7(ADAM32):c.1574C>T (p.Ser525Leu) | not specified [RCV004898972] | uncertain significance | 8 | 39232075 | 39232075 | Human | | name |
| 597778279 | CV3648344 | single nucleotide variant | NM_145004.7(ADAM32):c.1285G>A (p.Gly429Arg) | not specified [RCV004898977] | uncertain significance | 8 | 39221661 | 39221661 | Human | | name |
| 597738757 | CV3648363 | single nucleotide variant | NM_145004.7(ADAM32):c.1756T>A (p.Leu586Met) | not specified [RCV004890187] | uncertain significance | 8 | 39234020 | 39234020 | Human | | name |
| 597778583 | CV3648381 | single nucleotide variant | NM_145004.7(ADAM32):c.2065A>G (p.Ile689Val) | not specified [RCV004899005] | uncertain significance | 8 | 39257246 | 39257246 | Human | | name |
| 597778322 | CV3648392 | single nucleotide variant | NM_145004.7(ADAM32):c.1730C>A (p.Ser577Tyr) | not specified [RCV004899015] | uncertain significance | 8 | 39233994 | 39233994 | Human | | name |
| 598191952 | CV3943463 | single nucleotide variant | NM_145004.7(ADAM32):c.1355C>T (p.Pro452Leu) | not specified [RCV005312709] | uncertain significance | 8 | 39223068 | 39223068 | Human | | name |
| 598192055 | CV3943481 | single nucleotide variant | NM_145004.7(ADAM32):c.1216G>A (p.Asp406Asn) | not specified [RCV005312724] | uncertain significance | 8 | 39211307 | 39211307 | Human | | name |
