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Items: 1 to 20 of 268

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971659inversion1nstd209human GRCh38 chr17: 45,709,543-46,285,600 , GRCh37.p13 chr17: 43,786,909-44,362,966 CRHR1, MAPT, 14 more genes
    nsv5937206copy number variation1nstd209human GRCh38 chr17: 45,613,816-46,277,009 , GRCh37.p13 chr17: 43,691,182-44,354,375 LOC100132570, MAPT-IT1, 17 more genes
    nsv5672416inversion1nstd207human GRCh37.p13 chr17: 43,642,735-44,574,574 , GRCh38 chr17: 45,565,369-46,497,208 , CRHR1, 25 more genes
    nsv5669290inversion1nstd207human GRCh37.p13 chr17: 43,651,055-44,369,411 , GRCh38 chr17: 45,573,689-46,292,045 CRHR1, MAPT, 21 more genes
    nsv5559068sequence alteration1nstd206human GRCh38 chr17: 45,585,847-46,260,627 , GRCh37.p13 chr17: 43,663,213-44,337,993 KANSL1, MAPK8IP1P1, 19 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5391541copy number variation1nstd186human GRCh37 chr17: 43,655,785-44,366,714 , GRCh38.p12 chr17|NT_187663.1: 280,558-954,783 , GRCh38.p12 chr17: 45,578,419-46,289,348 LINC02210-CRHR1, STH, 22 more genes
    nsv5390044copy number variation1nstd186human GRCh37 chr17: 43,655,784-44,366,714 , GRCh38.p12 chr17|NT_187663.1: 280,557-954,783 , GRCh38.p12 chr17: 45,578,418-46,289,348 LOC100132570, KANSL1-AS1, 22 more genes
    nsv5381105copy number variation1nstd102humanUncertain significance GRCh37 chr17: 44,073,755-44,159,918 , GRCh38.p12 chr17|NT_187663.1: 698,508-784,653 , GRCh38.p12 chr17: 45,996,389-46,082,552 MAPT, STH, 1 more genes
    nsv5183821mobile element insertion1nstd203human GRCh38 chr17: 45,999,204-45,999,222 , GRCh37.p13 chr17: 44,076,570-44,076,588 MAPT, STH
    nsv5013755copy number variation1nstd200human GRCh38 chr17: 45,578,418-46,289,348 , GRCh37.p13 chr17: 43,655,784-44,366,714 DND1P2, MAPT-IT1, 21 more genes
    nsv4864680copy number variation1nstd200human GRCh37 chr17: 43,655,785-44,366,714 , GRCh38.p12 chr17|NT_187663.1: 280,558-954,783 , GRCh38.p12 chr17: 45,578,419-46,289,348 LOC107985027, KANSL1, 22 more genes
    nsv4729928copy number variation1nstd102humanPathogenic GRCh37 chr17: 43,586,396-44,212,416 , GRCh38.p12 chr17: 45,509,030-46,135,050 , GRCh38.p12 chr17|NT_187663.1: 199,185-837,157 SPPL2C, MAPT-IT1, 21 more genes
    nsv4727901copy number variation2nstd197human GRCh37 chr17: 43,515,225-44,249,509 , GRCh38.p12 chr17: 45,437,859-46,172,143 , GRCh38.p12 chr17|NT_187663.1: 128,364-874,248 CRHR1, MAPT, 24 more genes
    nsv4684193copy number variation1nstd102humanPathogenic GRCh37 chr17: 43,559,851-44,248,220 , GRCh38.p12 chr17|NT_187663.1: 172,640-872,959 , GRCh38.p12 chr17: 45,482,485-46,170,854 LOC105371800, KANSL1, 23 more genes
    nsv4676249copy number variation1nstd102humanPathogenic GRCh37 chr17: 43,655,356-44,784,639 , GRCh38.p12 chr17: 45,577,990-46,707,273 , GRCh38.p12 chr17|NT_187663.1: 280,129-1,226,699 KANSL1-AS1, LINC02210, 30 more genes
    nsv4657998inversion1nstd185human GRCh37.p13 chr17: 43,705,165-44,294,406 , GRCh38.p13 chr17: 45,627,799-46,217,040 CRHR1, MAPT, 13 more genes
    nsv4578253copy number variation1nstd102humanPathogenic GRCh37 chr17: 43,706,886-44,210,822 , GRCh38.p12 chr17: 45,629,520-46,133,456 , GRCh38.p12 chr17|NT_187663.1: 331,644-835,563 LOC107985028, LOC105371800, 11 more genes
    nsv4570999sequence alteration1nstd166human GRCh37.p13 chr17: 43,649,098-44,338,906 , GRCh38.p12 chr17: 45,571,732-46,261,540 , GRCh38.p12 chr17|NT_187663.1: 273,871-954,783 MAPT, SPPL2C, 20 more genes
    nsv4380004copy number variation1nstd173human GRCh37 chr17: 43,655,357-44,784,639 , GRCh38.p12 chr17: 45,577,991-46,707,273 , GRCh38.p12 chr17|NT_187663.1: 280,130-1,226,699 , STH, 31 more genes
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