slc9b2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4456563	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 103,900,089-103,940,328 , GRCh38.p12 chr4: 102,978,932-103,019,171	SLC9B2, SLC9B1
nsv7097220	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 101,947,022-106,061,534 , GRCh38.p12 chr4: 101,025,865-105,140,377	SLC9B2, LOC100419096, 41 more genes
nsv6311893	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr4: 101,947,022-104,640,832 , GRCh38.p12 chr4: 101,025,865-103,719,675	SLC9B2, LOC102723704, 32 more genes
nsv3873978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724	SLC9B2, LOC100422029, 2358 more genes
nsv3876533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611	SLC9B2, LOC100420289, 2347 more genes
nsv3884499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286	SLC9B2, MTND4LP29, 2341 more genes
nsv3880085	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318	SLC9B2, LOC112268460, 2345 more genes
nsv3883791	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495	SLC9B2, LOC105377343, 2341 more genes
nsv3875534	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 93,071,152-190,957,473 , GRCh38.p12 chr4: 92,150,001-190,036,318	SLC9B2, KLKB1, 1118 more genes
nsv6291432	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354	SLC9B2, SNHG27, 1091 more genes
nsv3920388	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 97,014,044-137,331,362 , NCBI36 chr4: 97,233,067-137,550,812 , GRCh38 chr4: 96,092,893-136,410,207	SLC9B2, MIR576, 447 more genes
nsv6315383	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 102,851,823-104,641,864 , GRCh38.p12 chr4: 101,930,666-103,720,707	SLC9B2, CENPE, 26 more genes
nsv6291428	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 95,490,755-109,977,216 , GRCh38.p12 chr4: 94,569,604-109,056,060	SLC9B2, ADH1A, 157 more genes
nsv4674207	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 103,865,132-105,720,367 , GRCh38.p12 chr4: 102,943,975-104,799,210	SLC9B2, TACR3, 11 more genes
nsv3878913	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 103,846,070-104,693,179 , GRCh38.p12 chr4: 102,924,913-103,772,022	SLC9B2, DDX3P3, 6 more genes
nsv7098788	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 101,947,022-107,268,849 , GRCh38.p12 chr4: 101,025,865-106,347,692	SLC9B2, LOC107986297, 60 more genes

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