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Items: 1 to 20 of 352

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137736copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,263,517-155,260,560 , GRCh38.p12 chrX: 153,998,066-156,030,895 H2AB3, GDI1, 83 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5968633copy number variation1nstd209human GRCh38 chrX: 154,751,108-154,757,229 , GRCh37.p13 chrX: 153,979,383-153,985,504 , GRCh37.p13 chrX|NW_003871103.3: 2,185,087-2,191,208 GAB3
    nsv5878993copy number variation1nstd209human GRCh38 chrX: 154,598,638-155,803,675 , GRCh37.p13 chrX|NW_003871103.3: 2,032,617-3,110,903 , GRCh37.p13 chrX: 153,826,899-154,906,585 MIR1184-2, TMLHE-AS1, 39 more genes
    nsv5878330copy number variation1nstd209human GRCh38 chrX: 154,709,891-154,710,144 , GRCh37.p13 chrX|NW_003871103.3: 2,143,870-2,144,123 , GRCh37.p13 chrX: 153,938,166-153,938,419 GAB3
    nsv5876904copy number variation1nstd209human GRCh38 chrX: 154,751,228-154,756,719 , GRCh37.p13 chrX: 153,979,503-153,984,994 , GRCh37.p13 chrX|NW_003871103.3: 2,185,207-2,190,698 GAB3
    nsv5875581copy number variation1nstd209human GRCh38 chrX: 154,709,160-154,710,083 , GRCh37.p13 chrX: 153,937,435-153,938,358 , GRCh37.p13 chrX|NW_003871103.3: 2,143,139-2,144,062 GAB3
    nsv5874785copy number variation1nstd209human GRCh38 chrX: 154,690,528-154,690,624 , GRCh37.p13 chrX|NW_003871103.3: 2,124,507-2,124,603 , GRCh37.p13 chrX: 153,918,803-153,918,899 GAB3
    nsv5872567copy number variation1nstd209human GRCh38 chrX: 154,710,048-154,710,098 , GRCh37.p13 chrX: 153,938,323-153,938,373 , GRCh37.p13 chrX|NW_003871103.3: 2,144,027-2,144,077 GAB3
    nsv5726123mobile element insertion2nstd211human GRCh38 chrX: 154,688,748-154,688,748 , GRCh37.p13 chrX: 153,917,023-153,917,023 , GRCh37.p13 chrX|NW_003871103.3: 2,122,727-2,122,727 GAB3
    nsv5431233copy number variation1nstd206human GRCh38 chrX: 154,710,024-154,710,159 , GRCh37.p13 chrX|NW_003871103.3: 2,144,003-2,144,138 , GRCh37.p13 chrX: 153,938,299-153,938,434 GAB3
    nsv5427222copy number variation1nstd206human GRCh38 chrX: 154,709,896-154,710,145 , GRCh37.p13 chrX|NW_003871103.3: 2,143,875-2,144,124 , GRCh37.p13 chrX: 153,938,171-153,938,420 GAB3
    nsv5422370copy number variation1nstd206human GRCh38 chrX: 154,739,674-154,739,782 , GRCh37.p13 chrX|NW_003871103.3: 2,173,653-2,173,761 , GRCh37.p13 chrX: 153,967,949-153,968,057 GAB3
    nsv5380363translocation1nstd200human GRCh38 chrX: 154,710,117-154,710,117 , GRCh38 chrX: 154,708,751-154,708,751 , GRCh37.p13 chrX|NW_003871103.3: 2,144,096-2,144,096 , GRCh37.p13 chrX: 153,937,026-153,937,026 , GRCh37.p13 chrX: 153,938,392-153,938,392 , GRCh37.p13 chrX|NW_003871103.3: 2,142,730-2,142,730 GAB3
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv4894192copy number variation1nstd200human GRCh38 chrX: 154,709,508-154,710,501 , GRCh37.p13 chrX: 153,937,783-153,938,776 , GRCh37.p13 chrX|NW_003871103.3: 2,143,487-2,144,480 GAB3
    nsv4787992copy number variation1nstd200human GRCh37 chrX: 153,962,238-153,964,225 , GRCh38.p12 chrX: 154,733,963-154,735,950 GAB3
    nsv4787991copy number variation1nstd200human GRCh37 chrX: 153,938,716-153,938,782 , GRCh38.p12 chrX: 154,710,441-154,710,507 GAB3
    nsv4787990copy number variation1nstd200human GRCh37 chrX: 153,937,783-153,938,776 , GRCh38.p12 chrX: 154,709,508-154,710,501 GAB3
    nsv4787989copy number variation1nstd200human GRCh37 chrX: 153,937,487-153,939,923 , GRCh38.p12 chrX: 154,709,212-154,711,648 GAB3
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