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Items: 1 to 20 of 299

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5911692copy number variation1nstd209human GRCh37.p13 chr7: 57,481,040-57,586,048 , GRCh38 chr7: 57,421,328-57,579,886 , GRCh37.p13 chr7|NW_003571038.1: 146,809-251,823 ZNF716, SAPCD2P2, 4 more genes
    nsv5847344copy number variation1nstd209human GRCh38 chr7: 57,465,124-57,469,066 , GRCh37.p13 chr7: 57,524,830-57,528,772 , GRCh37.p13 chr7|NW_003571038.1: 190,605-194,547 ZNF716
    nsv5847343copy number variation1nstd209human GRCh38 chr7: 57,460,474-57,477,716 , GRCh37.p13 chr7|NW_003571038.1: 185,955-203,197 , GRCh37.p13 chr7: 57,520,180-57,537,422 VN1R29P, ZNF716
    nsv5847014copy number variation1nstd209human GRCh37.p13 chr7|NW_003571038.1: 146,822-174,992 , GRCh38 chr7: 57,421,341-57,449,511 , GRCh37.p13 chr7: 57,481,053-57,509,217 ZNF716, SAPCD2P2, 1 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
    nsv5482153copy number variation1nstd206human GRCh38 chr7: 56,993,800-57,540,242 , GRCh37.p13 chr7: 57,190,580-57,599,948 , MTCYBP29, 39 more genes
    nsv5481609copy number variation1nstd206human GRCh38 chr7: 57,470,127-57,470,177 , GRCh37.p13 chr7|NW_003571038.1: 195,608-195,658 , GRCh37.p13 chr7: 57,529,833-57,529,883 ZNF716
    nsv5312845copy number variation1nstd204human GRCh37.p13 chr7|NW_003571038.1: 146,779-251,852 , GRCh37.p13 chr7: 57,481,010-57,586,077 , GRCh38.p13 chr7: 57,421,298-57,579,916 ZNF716, SAPCD2P2, 4 more genes
    nsv5233925copy number variation1nstd204human GRCh38.p13 chr7: 57,446,201-57,453,800 , GRCh37.p13 chr7: 57,505,907-57,513,506 , GRCh37.p13 chr7|NW_003571038.1: 171,682-179,281 ZNF716
    nsv5231120copy number variation1nstd204human GRCh38.p13 chr7: 57,463,527-57,489,727 , GRCh37.p13 chr7|NW_003571038.1: 189,008-215,208 , GRCh37.p13 chr7: 57,523,233-57,549,433 ZNF716, VN1R29P
    nsv5230836copy number variation1nstd204human GRCh38.p13 chr7: 57,461,449-57,475,916 , GRCh37.p13 chr7|NW_003571038.1: 186,930-201,397 , GRCh37.p13 chr7: 57,521,155-57,535,622 ZNF716, VN1R29P
    nsv5228075copy number variation1nstd204human GRCh38.p13 chr7: 57,468,217-57,470,916 , GRCh37.p13 chr7|NW_003571038.1: 193,698-196,397 , GRCh37.p13 chr7: 57,527,923-57,530,622 ZNF716
    nsv5225043copy number variation1nstd204human GRCh38.p13 chr7: 57,419,614-57,471,666 , GRCh37.p13 chr7|NW_003571038.1: 145,095-197,147 , GRCh37.p13 chr7: 57,479,326-57,531,372 SAPCD2P2, VN1R28P, 1 more genes
    nsv5224524copy number variation1nstd204human GRCh38.p13 chr7: 57,446,201-57,459,800 , GRCh37.p13 chr7|NW_003571038.1: 171,682-185,281 , GRCh37.p13 chr7: 57,505,907-57,519,506 ZNF716
    nsv5223728copy number variation1nstd204human GRCh38.p13 chr7: 57,465,475-57,487,853 , GRCh37.p13 chr7: 57,525,181-57,547,559 , GRCh37.p13 chr7|NW_003571038.1: 190,956-213,334 VN1R29P, ZNF716
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4964675copy number variation1nstd200human GRCh38 chr7: 57,185,639-57,823,153 , GRCh37.p13 chr7: 57,253,346-57,882,859 LOC105375297, GUSBP12, 27 more genes
    nsv4956908copy number variation1nstd200human GRCh38 chr7: 57,452,491-57,452,666 , GRCh37.p13 chr7|NW_003571038.1: 177,972-178,147 , GRCh37.p13 chr7: 57,512,197-57,512,372 ZNF716
    nsv4956891copy number variation1nstd200human GRCh38 chr7: 57,056,195-63,228,539 , GRCh37.p13 chr7: 57,190,578-62,688,917 , SEPTIN7P15, 50 more genes
    nsv4765725inversion1nstd199human GRCh37 chr7: 57,119,077-62,979,736 , GRCh38.p12 chr7: 57,051,370-63,519,358 , ZNF479, 70 more genes
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