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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097517copy number variation1nstd102humanUncertain significance GRCh37 chr5: 150,632,778-150,727,021 , GRCh38.p12 chr5: 151,253,217-151,347,460 ATP6V1G1P5, SLC36A3, 2 more genes
    nsv7096760copy number variation1nstd102humanUncertain significance GRCh37 chr5: 150,632,778-150,646,494 , GRCh38.p12 chr5: 151,253,217-151,266,933 GM2A
    nsv7053998inversion1nstd229human GRCh38 chr5: 148,749,982-154,424,819 , GRCh37.p13 chr5: 148,129,545-153,804,379 HMGXB3, RN7SL868P, 102 more genes
    nsv6784079copy number variation1nstd229human GRCh38 chr5: 151,238,885-151,301,466 , GRCh37.p13 chr5: 150,618,446-150,681,027 SLC36A3, GM2A
    nsv6781215copy number variation1nstd229human GRCh38 chr5: 151,269,818-151,287,337 , GRCh37.p13 chr5: 150,649,379-150,666,898 SLC36A3, GM2A
    nsv6778149copy number variation1nstd229human GRCh38 chr5: 151,245,914-151,331,227 , GRCh37.p13 chr5: 150,625,475-150,710,788 SLC36A3, SLC36A2, 2 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
    nsv6630065copy number variation1nstd224human GRCh37 chr5: 150,551,827-150,672,982 , GRCh38.p12 chr5: 151,172,266-151,293,421 SLC36A3, LOC105378230, 2 more genes
    nsv6571686inversion1nstd223human GRCh38 chr5: 151,260,544-151,261,503 , GRCh37.p13 chr5: 150,640,105-150,641,064 GM2A
    nsv6414028copy number variation1nstd223human GRCh38 chr5: 151,262,489-151,263,724 , GRCh37.p13 chr5: 150,642,050-150,643,285 GM2A
    nsv6404819copy number variation1nstd223human GRCh38 chr5: 151,257,275-151,257,701 , GRCh37.p13 chr5: 150,636,836-150,637,262 GM2A
    nsv6396610copy number variation1nstd223human GRCh38 chr5: 151,245,914-151,331,224 , GRCh37.p13 chr5: 150,625,475-150,710,785 ATP6V1G1P5, SLC36A2, 2 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
    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
    nsv6135120copy number variation1nstd213human GRCh37 chr5: 143,910,000-152,670,001 , GRCh38.p12 chr5: 144,530,437-153,290,441 ADRB2, ANXA6, 143 more genes
    nsv6009059copy number variation1nstd212human GRCh38 chr5: 151,261,636-151,261,769 , GRCh37.p13 chr5: 150,641,197-150,641,330 GM2A
    nsv5679548mobile element insertion1nstd211human GRCh38 chr5: 151,266,462-151,266,462 , GRCh37.p13 chr5: 150,646,023-150,646,023 GM2A
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4939209copy number variation1nstd200human GRCh38 chr5: 151,262,490-151,263,724 , GRCh37.p13 chr5: 150,642,051-150,643,285 GM2A
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