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Items: 1 to 20 of 948

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147712copy number variation1nstd232human GRCh37.p13 chr9: 136,638,023-136,638,096 , GRCh38.p12 chr9: 133,772,901-133,772,974 VAV2
    nsv7145184copy number variation1nstd232human GRCh37.p13 chr9: 136,692,559-136,692,613 , GRCh38.p12 chr9: 133,827,437-133,827,491 VAV2
    nsv7144313copy number variation1nstd232human GRCh37.p13 chr9: 136,693,395-136,693,585 , GRCh38.p12 chr9: 133,828,273-133,828,463 VAV2
    nsv7142574insertion1nstd232human GRCh37.p13 chr9: 136,779,933-136,779,933 , GRCh38.p12 chr9: 133,914,811-133,914,811 VAV2
    nsv7141061copy number variation1nstd232human GRCh37.p13 chr9: 136,693,442-136,693,585 , GRCh38.p12 chr9: 133,828,320-133,828,463 VAV2
    nsv7137739copy number variation1nstd232human GRCh37.p13 chr9: 136,657,066-136,657,139 , GRCh38.p12 chr9: 133,791,944-133,792,017 VAV2
    nsv7098066copy number variation4nstd102humanUncertain significance GRCh37 chr9: 135,139,626-140,034,216 , GRCh38.p12 chr9: 132,264,239-137,139,764 LINC02692, SNORD141A, 181 more genes
    nsv7097697copy number variation1nstd102humanUncertain significance GRCh37 chr9: 136,218,768-141,016,451 , GRCh38.p12 chr9: 133,351,913-138,121,999 LOC105376326, LOC107987143, 186 more genes
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv7075196inversion1nstd229human GRCh38 chr9: 130,990,409-137,053,229 , GRCh37.p13 chr9: 133,865,796-139,947,681 LINC02907, LCN1, 196 more genes
    nsv7073534inversion1nstd229human GRCh38 chr9: 133,787,806-133,787,911 , GRCh37.p13 chr9: 136,652,928-136,653,033 VAV2
    nsv7073297inversion1nstd229human GRCh38 chr9: 133,806,625-133,806,764 , GRCh37.p13 chr9: 136,671,747-136,671,886 VAV2
    nsv7068962inversion1nstd229human GRCh38 chr9: 133,882,906-133,883,047 , GRCh37.p13 chr9: 136,748,028-136,748,169 VAV2
    nsv7067679inversion1nstd229human GRCh38 chr9: 133,945,476-133,955,919 , GRCh37.p13 chr9: 136,810,598-136,821,041 VAV2
    nsv7064713inversion1nstd229human GRCh38 chr9: 133,859,472-133,859,522 , GRCh37.p13 chr9: 136,724,594-136,724,644 VAV2
    nsv7060209inversion1nstd229human GRCh38 chr9: 133,220,670-135,537,297 , GRCh37.p13 chr9: 136,369,193-138,429,143 COL5A1, DBH, 66 more genes
    nsv7059760inversion1nstd229human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 LCN10, RAPGEF1, 196 more genes
    nsv6897885copy number variation1nstd229human GRCh38 chr9: 133,815,632-133,974,078 , GRCh37.p13 chr9: 136,680,754-136,839,200 VAV2
    nsv6897816copy number variation1nstd229human GRCh38 chr9: 133,954,235-133,961,037 , GRCh37.p13 chr9: 136,819,357-136,826,159 VAV2
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