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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047362inversion1nstd229human GRCh38 chr5: 170,787,163-170,794,271 , GRCh37.p13 chr5: 170,214,167-170,221,275 GABRP
    nsv6793182copy number variation1nstd229human GRCh38 chr5: 170,796,401-170,801,000 , GRCh37.p13 chr5: 170,223,405-170,228,004 GABRP
    nsv6791642copy number variation1nstd229human GRCh38 chr5: 170,783,618-170,788,739 , GRCh37.p13 chr5: 170,210,622-170,215,743 GABRP
    nsv6786477copy number variation1nstd229human GRCh38 chr5: 170,783,876-170,788,572 , GRCh37.p13 chr5: 170,210,880-170,215,576 GABRP
    nsv6785518copy number variation1nstd229human GRCh38 chr5: 170,784,373-170,784,438 , GRCh37.p13 chr5: 170,211,377-170,211,442 GABRP
    nsv6781511copy number variation1nstd229human GRCh38 chr5: 170,662,244-174,111,903 , GRCh37.p13 chr5: 170,089,248-173,538,906 LOC101928093, LOC107986482, 79 more genes
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    nsv6636414copy number variation1nstd102humanUncertain significance GRCh37 chr5: 169,679,354-170,242,652 , GRCh38.p12 chr5: 170,252,350-170,815,648 GABRP, KCNIP1-OT1, 10 more genes
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6268177copy number variation1nstd214human GRCh38 chr5: 170,802,672-170,802,779 , GRCh37.p13 chr5: 170,229,676-170,229,783 GABRP
    nsv6220119insertion1nstd214human GRCh38 chr5: 170,784,373-170,784,373 , GRCh37.p13 chr5: 170,211,377-170,211,377 GABRP
    nsv6217448insertion1nstd214human GRCh38 chr5: 170,802,672-170,802,672 , GRCh37.p13 chr5: 170,229,676-170,229,676 GABRP
    nsv6182734copy number variation1nstd214human GRCh38 chr5: 170,802,741-170,802,793 , GRCh37.p13 chr5: 170,229,745-170,229,797 GABRP
    nsv6181639copy number variation1nstd214human GRCh38 chr5: 170,802,809-170,802,864 , GRCh37.p13 chr5: 170,229,813-170,229,868 GABRP
    nsv6136090copy number variation1nstd213human GRCh37 chr5: 161,030,000-172,600,001 , GRCh38.p12 chr5: 161,602,994-173,172,998 BNIP1, CCNG1, 130 more genes
    nsv6135392copy number variation1nstd213human GRCh37 chr5: 169,960,000-170,570,001 , GRCh38.p12 chr5: 170,532,996-171,142,997 GABRP, KCNIP1, 7 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6071376insertion1nstd212human GRCh38 chr5: 170,802,799-170,802,799 , GRCh37.p13 chr5: 170,229,803-170,229,803 GABRP
    nsv6069858insertion1nstd212human GRCh38 chr5: 170,802,834-170,802,834 , GRCh37.p13 chr5: 170,229,838-170,229,838 GABRP
    nsv6014008copy number variation1nstd212human GRCh38 chr5: 170,802,747-170,802,801 , GRCh37.p13 chr5: 170,229,751-170,229,805 GABRP
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