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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098788copy number variation1nstd102humanUncertain significance GRCh37 chr4: 101,947,022-107,268,849 , GRCh38.p12 chr4: 101,025,865-106,347,692 LOC107986297, LOC100288914, 60 more genes
    nsv7097220copy number variation1nstd102humanPathogenic GRCh37 chr4: 101,947,022-106,061,534 , GRCh38.p12 chr4: 101,025,865-105,140,377 LOC100419096, LOC105377347, 41 more genes
    nsv7096485copy number variation1nstd102humanPathogenic GRCh37 chr4: 102,001,669-103,806,607 , GRCh38.p12 chr4: 101,080,512-102,885,450 SLC9B1, MIR8066, 24 more genes
    nsv7054609inversion1nstd229human GRCh38 chr4: 95,257,712-104,152,159 , GRCh37.p13 chr4: 96,178,863-105,073,316 SLC39A8, PABPC1P7, 96 more genes
    nsv7052845inversion1nstd229human GRCh38 chr4: 97,450,222-102,053,198 , GRCh37.p13 chr4: 98,371,373-102,974,355 RNU6-462P, LOC105377345, 58 more genes
    nsv7052661inversion1nstd229human GRCh38 chr4: 96,912,053-103,991,076 , GRCh37.p13 chr4: 97,833,204-104,912,233 MIR1255A, LOC107986297, 86 more genes
    nsv7048086inversion1nstd229human GRCh38 chr4: 100,058,481-107,564,371 , GRCh37.p13 chr4: 100,979,638-108,485,528 ACTR6P1, INTS12, 79 more genes
    nsv7046928inversion1nstd229human GRCh38 chr4: 95,051,434-103,882,549 , GRCh37.p13 chr4: 95,972,585-104,803,706 PABPC1P7, RN7SL728P, 95 more genes
    nsv7044544inversion1nstd229human GRCh38 chr4: 98,964,941-108,185,877 , GRCh37.p13 chr4: 99,886,092-109,107,033 LOC102725220, TACR3, 117 more genes
    nsv6744651copy number variation1nstd229human GRCh38 chr4: 101,134,711-101,527,569 , GRCh37.p13 chr4: 102,055,868-102,448,726 MIR1255A, PPP3CA, 2 more genes
    nsv6629273copy number variation1nstd224human GRCh37 chr4: 102,239,170-102,783,776 , GRCh38.p12 chr4: 101,318,013-101,862,619 PPP3CA, BANK1, 4 more genes
    nsv6382480copy number variation1nstd223human GRCh38 chr4: 101,134,711-101,527,569 , GRCh37.p13 chr4: 102,055,868-102,448,726 MIR8066, FLJ20021, 2 more genes
    nsv6311893copy number variation2nstd102humanPathogenic GRCh37 chr4: 101,947,022-104,640,832 , GRCh38.p12 chr4: 101,025,865-103,719,675 LOC102723704, BDH2, 32 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6291428copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 95,490,755-109,977,216 , GRCh38.p12 chr4: 94,569,604-109,056,060 ADH1A, ADH1B, 157 more genes
    nsv6135624copy number variation1nstd213human GRCh37 chr4: 94,300,000-108,550,001 , GRCh38.p12 chr4: 93,378,849-107,628,845 , ADH1A, 146 more genes
    nsv6135091copy number variation1nstd213human GRCh37 chr4: 94,310,000-108,550,001 , GRCh38.p12 chr4: 93,388,849-107,628,845 , ADH1A, 146 more genes
    nsv6134881copy number variation1nstd213human GRCh37 chr4: 101,940,000-102,270,001 , GRCh38.p12 chr4: 101,018,843-101,348,844 PPP3CA, FLJ20021, 2 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
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