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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7098892copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387 CIB1, RPS12P26, 326 more genes
    nsv6973832copy number variation1nstd229human GRCh38 chr15: 92,706,571-92,777,965 , GRCh37.p13 chr15: 93,249,801-93,321,195 RPL31P6, HMGN1P38, 3 more genes
    nsv6973254copy number variation1nstd229human GRCh38 chr15: 92,697,169-92,736,441 , GRCh37.p13 chr15: 93,240,399-93,279,671 FAM174B, H2AZ2P1, 2 more genes
    nsv6966620copy number variation1nstd229human GRCh38 chr15: 92,726,301-92,749,800 , GRCh37.p13 chr15: 93,269,531-93,293,030 FAM174B, H2AZ2P1
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
    nsv6511426copy number variation1nstd223human GRCh38 chr15: 92,730,593-92,775,010 , GRCh37.p13 chr15: 93,273,823-93,318,240 FTLP20, H2AZ2P1, 1 more genes
    nsv6506680copy number variation1nstd223human GRCh38 chr15: 92,713,829-92,777,033 , GRCh37.p13 chr15: 93,257,059-93,320,263 RPL31P6, FTLP20, 2 more genes
    nsv6499899copy number variation1nstd223human GRCh38 chr15: 92,718,174-92,733,167 , GRCh37.p13 chr15: 93,261,404-93,276,397 FAM174B, RPL31P6, 1 more genes
    nsv6499005copy number variation1nstd223human GRCh38 chr15: 92,730,583-92,731,675 , GRCh37.p13 chr15: 93,273,813-93,274,905 H2AZ2P1, FAM174B
    nsv6291795copy number variation1nstd102humanPathogenic GRCh37 chr15: 89,520,451-93,926,491 , GRCh38.p12 chr15: 88,977,220-93,383,262 LINC00930, TRY-GTA12-1, 106 more genes
    nsv6290316copy number variation1nstd102humanPathogenic GRCh37 chr15: 88,465,861-94,411,846 , GRCh38.p12 chr15: 87,922,630-93,868,617 LOC105370964, MRPL46, 130 more genes
    nsv6133155copy number variation1nstd213human GRCh37 chr15: 72,730,000-102,440,001 , GRCh38.p12 chr15: 72,437,659-101,899,798 , BLM, 609 more genes
    nsv6132919copy number variation1nstd213human GRCh37 chr15: 91,580,000-100,660,001 , GRCh38.p12 chr15: 91,036,770-100,119,796 ST8SIA2, SYNM, 116 more genes
    nsv6132917copy number variation1nstd213human GRCh37 chr15: 90,230,000-95,470,001 , GRCh38.p12 chr15: 89,686,769-94,926,772 BLM, ST8SIA2, 101 more genes
    nsv6112780copy number variation1nstd102humanPathogenic GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538 LOC105371009, ST8SIA2, 149 more genes
    nsv6023952copy number variation1nstd212human GRCh38 chr15: 92,732,146-92,733,042 , GRCh37.p13 chr15: 93,275,376-93,276,272 H2AZ2P1, FAM174B
    nsv5531067copy number variation1nstd206human GRCh38 chr15: 92,402,520-97,547,707 , GRCh37.p13 chr15: 92,945,750-98,090,937 , LOC105371004, 71 more genes
    nsv5514392copy number variation1nstd206human GRCh38 chr15: 92,730,301-92,732,803 , GRCh37.p13 chr15: 93,273,531-93,276,033 H2AZ2P1, FAM174B
    nsv5009192copy number variation1nstd200human GRCh38 chr15: 92,730,520-92,732,360 , GRCh37.p13 chr15: 93,273,750-93,275,590 FAM174B, H2AZ2P1
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