| 150439153 | CV1274966 | single nucleotide variant | NM_013964.5(NRG1):c.1062-5C>T | NRG1-related disorder [RCV003968492]|Schizophrenia 6 [RCV003994321]|not provided [RCV004707681]|not specified [RCV001703267] | benign|likely benign | 8 | 32760195 | 32760195 | Human | 1 | name , trait , alternate_id |
| 405293269 | CV3207353 | single nucleotide variant | NM_013964.5(NRG1):c.1062-4G>A | NRG1-related disorder [RCV003931741] | benign | 8 | 32760196 | 32760196 | Human | | name , trait , alternate_id |
| 8650249 | CV126824 | single nucleotide variant | NM_013962.2(NRG1):c.745+19828T>C | Lung cancer [RCV000107311] | uncertain significance | 8 | 31660557 | 31660557 | Human | | name |
| 151235967 | CV1319395 | single nucleotide variant | NM_001159995.3(NRG1):c.37+725G>A | not provided [RCV001797340] | benign | 8 | 31640156 | 31640156 | Human | | name |
| 10449778 | CV215383 | single nucleotide variant | NM_013964.5(NRG1):c.502+31229G>C | not provided [RCV004706660]|not specified [RCV000202884] | likely benign | 8 | 32648114 | 32648114 | Human | | name |
| 401925792 | CV2821013 | single nucleotide variant | NM_013964.5(NRG1):c.502+31211G>C | NRG1-related disorder [RCV003966430]|not provided [RCV003436852] | benign|likely benign | 8 | 32648096 | 32648096 | Human | 1 | name , trait , alternate_id |
| 405290447 | CV3200888 | single nucleotide variant | NM_013964.5(NRG1):c.502+30968G>A | NRG1-related disorder [RCV003984552] | benign | 8 | 32647853 | 32647853 | Human | | name , trait , alternate_id |
| 405284244 | CV3213663 | single nucleotide variant | NM_013964.5(NRG1):c.502+30933C>A | NRG1-related disorder [RCV003922231] | benign | 8 | 32647818 | 32647818 | Human | | name , trait , alternate_id |
| 408367431 | CV3512404 | single nucleotide variant | NM_013964.5(NRG1):c.502+31342G>A | NRG1-related disorder [RCV004758473] | likely benign | 8 | 32648227 | 32648227 | Human | | name , trait , alternate_id |
| 8650250 | CV126825 | single nucleotide variant | NM_013962.2(NRG1):c.745+100047C>A | Lung cancer [RCV000107312] | uncertain significance | 8 | 31740776 | 31740776 | Human | | name |
| 8650251 | CV126826 | single nucleotide variant | NM_013962.2(NRG1):c.745+146561G>C | Lung cancer [RCV000107313] | uncertain significance | 8 | 31787290 | 31787290 | Human | | name |
| 8650252 | CV126827 | single nucleotide variant | NM_013962.2(NRG1):c.746-399477C>T | Lung cancer [RCV000107314] | uncertain significance | 8 | 32196353 | 32196353 | Human | | name |
| 8650253 | CV126828 | single nucleotide variant | NM_013962.2(NRG1):c.746-139686A>G | Lung cancer [RCV000107315] | uncertain significance | 8 | 32456144 | 32456144 | Human | | name |
| 405275970 | CV3208219 | single nucleotide variant | NM_013962.3(NRG1):c.15C>G (p.Arg5=) | NRG1-related disorder [RCV003941656] | likely benign | 8 | 31639999 | 31639999 | Human | | name , trait , alternate_id |
| 8644866 | CV104273 | single nucleotide variant | NM_013962.3(NRG1):c.11G>A (p.Arg4Gln) | NRG1-related disorder [RCV003952532]|not provided [RCV000084671] | benign|not provided | 8 | 31639995 | 31639995 | Human | 1 | name , trait , alternate_id |
| 8644868 | CV104275 | single nucleotide variant | NM_013962.3(NRG1):c.26G>A (p.Arg9His) | NRG1-related disorder [RCV003952533]|not provided [RCV000084673] | benign|likely benign|not provided | 8 | 31640010 | 31640010 | Human | 1 | name , trait , alternate_id |
| 405286764 | CV3213811 | single nucleotide variant | NM_013964.5(NRG1):c.111C>G (p.Pro37=) | NRG1-related disorder [RCV003924208] | likely benign | 8 | 32595838 | 32595838 | Human | | name , trait , alternate_id |
| 15162705 | CV751109 | single nucleotide variant | NM_013964.5(NRG1):c.141G>A (p.Ser47=) | not provided [RCV000925950] | benign | 8 | 32595868 | 32595868 | Human | | name |
| 15160566 | CV751110 | single nucleotide variant | NM_013964.5(NRG1):c.162C>T (p.Val54=) | not provided [RCV000925510] | likely benign | 8 | 32595889 | 32595889 | Human | | name |
| 15104827 | CV751111 | single nucleotide variant | NM_013964.5(NRG1):c.282G>A (p.Lys94=) | not provided [RCV000915426] | likely benign | 8 | 32605565 | 32605565 | Human | | name |
| 8644876 | CV104283 | single nucleotide variant | NM_013964.5(NRG1):c.30A>C (p.Lys10Asn) | not provided [RCV000084681] | not provided | 8 | 32548756 | 32548756 | Human | | name |
| 15115508 | CV711502 | single nucleotide variant | NM_013964.5(NRG1):c.414T>C (p.Gly138=) | NRG1-related disorder [RCV003905840]|not provided [RCV000961861] | benign | 8 | 32614527 | 32614527 | Human | 1 | name , trait , alternate_id |
| 15109681 | CV751112 | single nucleotide variant | NM_013964.5(NRG1):c.600A>G (p.Lys200=) | not provided [RCV000916384] | likely benign | 8 | 32728046 | 32728046 | Human | | name |
| 8644877 | CV104284 | single nucleotide variant | NM_013964.5(NRG1):c.140C>T (p.Ser47Leu) | not provided [RCV000084682] | not provided | 8 | 32595867 | 32595867 | Human | | name |
| 8644883 | CV104290 | single nucleotide variant | NM_013964.5(NRG1):c.1005T>C (p.Ser335=) | not provided [RCV000084688] | not provided | 8 | 32759380 | 32759380 | Human | | name |
| 405275760 | CV3197045 | single nucleotide variant | NM_013964.5(NRG1):c.113G>A (p.Arg38Gln) | NRG1-related disorder [RCV003974300] | benign | 8 | 32595840 | 32595840 | Human | | name , trait , alternate_id |
| 405278236 | CV3217201 | single nucleotide variant | NM_013962.3(NRG1):c.224T>C (p.Leu75Pro) | NRG1-related disorder [RCV003964375] | benign | 8 | 31640208 | 31640208 | Human | | name , trait , alternate_id |
| 15177429 | CV723059 | single nucleotide variant | NM_013964.5(NRG1):c.1365C>T (p.Pro455=) | NRG1-related disorder [RCV003930628]|not provided [RCV000884820] | benign | 8 | 32763844 | 32763844 | Human | 1 | name , trait , alternate_id |
| 15166119 | CV751113 | single nucleotide variant | NM_013964.5(NRG1):c.1095C>T (p.Ser365=) | not provided [RCV000926791] | likely benign | 8 | 32760233 | 32760233 | Human | | name |
| 15153541 | CV751114 | single nucleotide variant | NM_013964.5(NRG1):c.1104C>T (p.His368=) | not provided [RCV000924079] | likely benign | 8 | 32760242 | 32760242 | Human | | name |
| 15103229 | CV751115 | single nucleotide variant | NM_013964.5(NRG1):c.1380G>A (p.Thr460=) | NRG1-related disorder [RCV003978001]|not provided [RCV000915123] | likely benign | 8 | 32763859 | 32763859 | Human | 1 | name , trait , alternate_id |
| 15139626 | CV783098 | single nucleotide variant | NM_013964.5(NRG1):c.1158G>T (p.Gly386=) | not provided [RCV000982671] | likely benign | 8 | 32760296 | 32760296 | Human | | name |
| 21069729 | CV796166 | single nucleotide variant | NM_013964.5(NRG1):c.233A>T (p.Asn78Ile) | not provided [RCV000999022]|not specified [RCV004030248] | uncertain significance | 8 | 32595960 | 32595960 | Human | | name |
| 8632985 | CV88200 | single nucleotide variant | NM_013956.3(NRG1):c.1797C>T (p.Pro599=) | Malignant melanoma [RCV000068292] | not provided | 8 | 32764261 | 32764261 | Human | | name |
| 8644878 | CV104285 | single nucleotide variant | NM_013964.5(NRG1):c.679A>G (p.Met227Val) | not provided [RCV000084683] | not provided | 8 | 32742054 | 32742054 | Human | | name |
| 8644879 | CV104286 | single nucleotide variant | NM_013964.5(NRG1):c.819G>T (p.Lys273Asn) | not provided [RCV000084684] | not provided | 8 | 32756418 | 32756418 | Human | | name |
| 8644880 | CV104287 | single nucleotide variant | NM_013964.5(NRG1):c.835C>G (p.Arg279Gly) | not provided [RCV000084685] | not provided | 8 | 32756434 | 32756434 | Human | | name |
| 8644881 | CV104288 | single nucleotide variant | NM_013964.5(NRG1):c.857G>A (p.Arg286Gln) | not provided [RCV000084686] | not provided | 8 | 32756456 | 32756456 | Human | | name |
| 8644882 | CV104289 | single nucleotide variant | NM_013964.5(NRG1):c.893A>G (p.His298Arg) | not provided [RCV000084687] | not provided | 8 | 32756492 | 32756492 | Human | | name |
| 127286022 | CV1053912 | single nucleotide variant | NM_013964.5(NRG1):c.332T>C (p.Met111Thr) | Hereditary spastic paraplegia [RCV001376152] | affects | 8 | 32605615 | 32605615 | Human | 1 | name |
| 150439734 | CV1274943 | single nucleotide variant | NM_013964.5(NRG1):c.781G>T (p.Val261Leu) | not provided [RCV004706246]|not specified [RCV001703389] | benign|likely benign | 8 | 32754452 | 32754452 | Human | | name |
| 405287716 | CV3217922 | single nucleotide variant | NM_013964.5(NRG1):c.866T>C (p.Met289Thr) | NRG1-related disorder [RCV003982045] | benign | 8 | 32756465 | 32756465 | Human | | name , trait , alternate_id |
| 405279635 | CV3221841 | single nucleotide variant | NM_013962.3(NRG1):c.473C>T (p.Ala158Val) | NRG1-related disorder [RCV003976406] | benign | 8 | 31640457 | 31640457 | Human | | name , trait , alternate_id |
| 8644884 | CV104291 | single nucleotide variant | NM_013964.5(NRG1):c.1322C>T (p.Thr441Met) | not provided [RCV000084689] | not provided | 8 | 32763801 | 32763801 | Human | | name |
| 8644885 | CV104292 | single nucleotide variant | NM_013964.5(NRG1):c.1538C>T (p.Pro513Leu) | not provided [RCV000084690] | not provided | 8 | 32764017 | 32764017 | Human | | name |
| 150435730 | CV1274858 | single nucleotide variant | NM_013964.5(NRG1):c.1633C>T (p.Arg545Trp) | not provided [RCV001702147]|not specified [RCV001726670] | benign|likely benign | 8 | 32764112 | 32764112 | Human | | name |
| 405284533 | CV3196947 | single nucleotide variant | NM_013964.5(NRG1):c.1847G>T (p.Gly616Val) | NRG1-related disorder [RCV003979793] | benign | 8 | 32764326 | 32764326 | Human | | name , trait , alternate_id |
| 405293219 | CV3207323 | single nucleotide variant | NM_013964.5(NRG1):c.1096G>A (p.Glu366Lys) | NRG1-related disorder [RCV003931712] | benign | 8 | 32760234 | 32760234 | Human | | name , trait , alternate_id |
| 405292840 | CV3210416 | single nucleotide variant | NM_013964.5(NRG1):c.1640C>T (p.Ala547Val) | NRG1-related disorder [RCV003931384] | likely benign | 8 | 32764119 | 32764119 | Human | | name , trait , alternate_id |
| 405283878 | CV3213388 | single nucleotide variant | NM_013964.5(NRG1):c.1808C>A (p.Pro603His) | NRG1-related disorder [RCV003921976] | benign | 8 | 32764287 | 32764287 | Human | | name , trait , alternate_id |
| 15153859 | CV711503 | single nucleotide variant | NM_013964.5(NRG1):c.1634G>A (p.Arg545Gln) | NRG1-related disorder [RCV003972880]|not provided [RCV000968623] | benign | 8 | 32764113 | 32764113 | Human | 1 | name , trait , alternate_id |
| 15168163 | CV736630 | single nucleotide variant | NM_013964.5(NRG1):c.1232C>G (p.Thr411Ser) | NRG1-related disorder [RCV003910808]|not provided [RCV000904797] | benign|likely benign | 8 | 32760370 | 32760370 | Human | 1 | name , trait , alternate_id |
| 21069731 | CV796167 | single nucleotide variant | NM_013964.5(NRG1):c.1246C>T (p.Arg416Ter) | not provided [RCV000999023] | uncertain significance | 8 | 32760384 | 32760384 | Human | | name |
| 405273959 | CV3207014 | microsatellite | NM_013962.3(NRG1):c.302CGG[4] (p.Ala105del) | NRG1-related disorder [RCV003919568] | likely benign | 8 | 31640284 | 31640286 | Human | | name , trait , alternate_id |
