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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098938copy number variation1nstd102humanUncertain significance GRCh38 chr7: 116,868,268-117,565,389 , GRCh37.p13 chr7: 116,508,322-117,205,443 ST7-AS1, MTND2P37, 20 more genes
    nsv6834517copy number variation1nstd229human GRCh38 chr7: 116,953,331-116,953,890 , GRCh37.p13 chr7: 116,593,385-116,593,944 ST7-OT4, ST7, 1 more genes
    nsv6833978copy number variation1nstd229human GRCh38 chr7: 116,923,492-117,035,471 , GRCh37.p13 chr7: 116,563,546-116,675,525 ST7, TPM3P1, 5 more genes
    nsv6831475copy number variation1nstd229human GRCh38 chr7: 110,527,230-117,297,230 , GRCh37.p13 chr7: 110,167,287-116,937,284 IMMP2L, LOC105375466, 66 more genes
    nsv6827180copy number variation1nstd229human GRCh38 chr7: 116,747,495-117,319,278 , GRCh37.p13 chr7: 116,387,549-116,959,332 LOC105375467, CAPZA2, 16 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6631746copy number variation1nstd224human GRCh37 chr7: 116,567,649-116,593,611 , GRCh38.p12 chr7: 116,927,595-116,953,557 ST7, ST7-AS1, 3 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6314995copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 114,885,745-124,728,629 , GRCh38.p12 chr7: 115,245,691-125,088,575 CAPZA2, CAV1, 109 more genes
    nsv6313851copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,984,287-128,949,489 , GRCh38.p12 chr7: 107,343,842-129,309,648 DOCK4-AS1, RPL3P8, 262 more genes
    nsv6313576copy number variation1nstd102humanPathogenic GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106 LHFPL3-AS2, CTB-30L5.1, 233 more genes
    nsv6305541copy number variation1nstd186human GRCh37 chr7: 116,555,644-116,607,061 , GRCh38.p12 chr7: 116,915,590-116,967,007 CAPZA2, ST7, 4 more genes
    nsv6303006copy number variation1nstd186human GRCh37 chr7: 116,545,440-116,696,425 , GRCh38.p12 chr7: 116,905,386-117,056,371 CAPZA2, ST7, 6 more genes
    nsv6136542copy number variation1nstd213human GRCh37 chr7: 116,240,000-116,990,001 , GRCh38.p12 chr7: 116,599,946-117,349,947 ST7-AS1, ST7-OT4, 17 more genes
    nsv6136533copy number variation1nstd213human GRCh37 chr7: 104,130,000-120,060,001 , GRCh38.p12 chr7: 104,489,552-120,419,947 CAPZA2, CFTR, 162 more genes
    nsv6135954copy number variation1nstd213human GRCh37 chr7: 114,370,000-117,780,001 , GRCh38.p12 chr7: 114,729,945-118,139,947 TFEC, TES, 40 more genes
    nsv6135874copy number variation1nstd213human GRCh37 chr7: 114,410,000-116,840,001 , GRCh38.p12 chr7: 114,769,945-117,199,947 CAV1, ST7-OT3, 27 more genes
    nsv6135872copy number variation1nstd213human GRCh37 chr7: 113,230,000-128,010,001 , GRCh38.p12 chr7: 113,589,945-128,369,947 CAV1, SLC13A1, 154 more genes
    nsv6017371copy number variation1nstd212human GRCh37.p13 chr7: 116,555,645-116,607,062 , GRCh38 chr7: 116,915,591-116,967,008 CAPZA2, ST7, 4 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
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